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Course 3 in the Optimal Medicine Series

Advancing Chronic Disease Care: From Root Cause to Resolution

November 6-8, 2026 • Salt Lake City, UT 

Metabolic & Inflammatory Health

Address the top seven chronic diseases affecting Americans today. Learn how BHRT, nutrition, and lifestyle interventions can work together to move from symptom management to lasting resolution and improved quality of life.

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Details

Course Description

Chronic diseases are often diagnosed and treated as separate conditions, yet obesity, diabetes, cardiovascular disease, cognitive decline, osteoporosis, sarcopenia, and other disorders frequently share common underlying drivers. Course 3 challenges providers to look beyond the diagnosis and rethink chronic disease through the interconnected roles of insulin resistance, hormonal decline, inflammation, visceral adiposity, muscle loss, and metabolic dysfunction.

Beginning with the physiology of insulin and nutrient signaling, participants will learn how metabolic dysfunction can develop years before traditional markers of disease become abnormal—and how earlier recognition may create opportunities for more meaningful intervention. The course then applies this framework to some of the most common and consequential chronic conditions encountered in practice, including obesity and diabetes, cardiovascular disease, obstructive sleep apnea, cognitive decline, osteoporosis, and sarcopenia.

Throughout the course, emphasis is placed on translating physiology and evidence into better patient care. Providers will explore practical approaches to assessment, laboratory interpretation, hormone optimization, metabolic interventions, nutrition, pharmacologic therapies, and other strategies that address underlying contributors to disease rather than focusing exclusively on downstream symptoms or diagnoses.

Participants will leave with a more integrated framework for evaluating patients with chronic disease—helping them recognize connections across seemingly different conditions, identify metabolic and hormonal dysfunction earlier, and develop more individualized strategies aimed at improving long-term health and function.

Upon completion of this course, participants should be able to:

  • Identify key upstream drivers of chronic disease, including insulin resistance, hormonal decline, visceral adiposity, loss of muscle, and metabolic dysfunction.
  • Evaluate metabolic and hormonal factors that may contribute to obesity, diabetes, cardiovascular disease, cognitive decline, sleep apnea, osteoporosis, and sarcopenia.
  • Interpret clinical and laboratory markers to recognize insulin resistance and metabolic dysfunction earlier in the disease process.
  • Apply evidence-based hormonal, metabolic, and pharmacologic strategies to address underlying contributors to chronic disease.
  • Develop more individualized treatment approaches that move beyond managing isolated diagnoses toward improving metabolic health, function, and long-term patient outcomes.

Agenda

Time (MT)Agenda
8:00 - 9:00 am

Beyond the Diagnosis: Rethinking Chronic Disease at Its Roots
Chronic diseases are traditionally taught and treated as distinct conditions—diabetes, cardiovascular disease, obesity, cognitive decline, osteoporosis, and others—yet many share interconnected upstream drivers. This opening session introduces a new framework for understanding chronic disease by looking beyond the diagnosis to the underlying processes that contribute to disease development and progression. Rather than approaching each condition in isolation, this session will explore six interconnected drivers of chronic disease: hyperinsulinemia, hormone decline, chronic inflammation, mitochondrial dysfunction, loss of muscle, and visceral adiposity. Providers will examine how these processes interact, reinforce one another, and contribute to multiple disease states—and how identifying and addressing them can shift care from downstream disease management toward earlier, root-cause intervention.

Faculty: Micah Olson, MD

9:00 - 10:00 amInsulin Physiology 101: Understanding a Key Driver of Chronic Disease
Insulin is often viewed primarily through the lens of glucose regulation, but its physiologic role extends far beyond blood sugar. As a powerful anabolic and storage hormone, insulin signals energy abundance, influences nutrient storage and utilization, supports growth, and suppresses the breakdown of stored energy and tissue. This session will review the physiology of insulin and establish the foundation for understanding what happens when this essential signaling system becomes chronically elevated or dysregulated. Providers will explore insulin's roles in energy availability, anabolism, storage, and anti-catabolic signaling—creating the physiologic foundation for the discussions of hyperinsulinemia, insulin resistance, obesity, diabetes, and chronic disease that follow.

Faculty: Micah Olson, MD

10:00 - 10:30 amBreak
10:30 - 12:30 pmNutrient Signaling: How Metabolism Shapes Health and Chronic Disease
Food provides more than energy. Nutrients—including glucose, fats, amino acids, and vitamins—act as signals that influence metabolism, insulin response, inflammation, cellular growth and repair, and hormone regulation. This session explores how the body senses and responds to nutrients through key metabolic hormones, including insulin, GIP, GLP-1, amylin, ghrelin, and glucagon, and the signaling pathways that coordinate these responses.

Providers will examine how healthy nutrient signaling maintains metabolic balance and what happens when these systems begin to break down, including impaired signaling and receptor resistance in tissues such as the liver. The session will connect disruptions in nutrient signaling to insulin resistance, metabolic dysfunction, and the development and progression of chronic disease.

Faculty: Micah Olson, MD

12:30 - 1:30 pmLunch
1:30 - 2:30 pmWhat is Insulin Resistance and Where Does it Come From?
This lecture defines insulin resistance at the level of the cell and the whole body, establishing that the condition cannot exist without hyperinsulinemia and that insulin is elevated for years while glucose remains normal. It then covers the three causes: stress, inflammation, and insulin itself, with evidence from sleep deprivation, air pollution, and carbohydrate overfeeding studies. The lecture closes by distinguishing pathological insulin resistance from the physiological insulin resistance of puberty, pregnancy, and the luteal phase, making the case that insulin resistance often begins as a protective adaptation.

Faculty: Ben Bikman, PhD

2:30 - 3:30 pmHow Does Insulin Resistance Contribute to Chronic Disease?
This lecture begins with why insulin resistance goes undetected, tracing the historical and practical reasons clinicians measure glucose rather than insulin, and showing that insulin resistance is identifiable decades before glucose rises. It then follows the disorder into specific tissues and diseases: the muscle, liver, and pancreatic alpha and beta cells in type 2 diabetes; cerebral fuel disruption in Alzheimer’s disease; and even how insulin resistance may lead to some not making adequate GLP-1.

Faculty: Ben Bikman, PhD

3:30 - 3:45 pmBreak
3:45 - 4:45 pmWhat Can We Do to Prevent or Reverse Insulin Resistance?
This lecture opens with assessment, comparing dynamic and static measures including the two hour OGTT with insulin, fasting insulin with C peptide, HOMA IR, the triglyceride to HDL ratio, and clinical signs such as acanthosis nigricans and waist to height ratio. It then evaluates pharmacological options against a single standard, whether the therapy lowers insulin, covering insulin therapy, sulfonylureas, metformin, and GLP-1 receptor agonists. The lecture ends with dietary strategy built on controlling carbohydrates, prioritizing protein, and not fearing fat, plus specific targets attendees can act on.

Faculty: Ben Bikman, PhD

4:45 - 5:15 pmQuestion and Answer

5:15 - 5:30 pm Book Signing with Ben

Time (MT)Agenda
8:00 - 10:00 amObesity and Diabetes: Beyond Calories to Metabolic Health
Obesity and type 2 diabetes are complex metabolic diseases that extend far beyond excess calories, body weight, or elevated glucose. This session examines the interconnected metabolic and hormonal processes that contribute to their development, including insulin resistance and hyperinsulinemia, visceral adiposity, inflammation, altered nutrient signaling, loss of metabolic flexibility, and changes in muscle and energy metabolism.

Providers will explore how these underlying dysfunctions can precede overt disease and why improving metabolic health requires looking beyond weight and glucose alone. The discussion will connect assessment and treatment strategies to the broader upstream drivers of chronic disease, providing a framework for addressing metabolic dysfunction and improving long-term health.

Faculty: Jason Giffi, MD

10:00 - 10:30 amBreak
10:30 - 12:00 pmHow Hormones Impact Obesity and Insulin Resistance
Obesity and insulin resistance are influenced by more than caloric intake and physical activity. Hormones play a critical role in regulating glucose metabolism, insulin sensitivity, body composition, fat distribution, energy expenditure, and the balance between anabolic and catabolic states.

This session examines how estradiol, testosterone, thyroid hormones, cortisol, and DHEA influence metabolic health and how hormonal decline or dysregulation may contribute to visceral adiposity, loss of lean mass, impaired glucose regulation, and insulin resistance. Participants will learn to recognize hormonal contributors to metabolic dysfunction and consider hormone optimization as part of a more comprehensive approach to improving metabolic health.

Faculty: Jason Giffi, MD

12:00 - 1:00 pmLunch
1:00 - 2:30 pmCardiovascular Disease: Beyond Cholesterol to Root Cause
Cardiovascular disease remains the leading cause of death worldwide, yet traditional approaches often focus primarily on cholesterol management rather than the underlying drivers of vascular disease. This session explores the role of insulin resistance, atherosclerosis, apolipoproteins, and inflammation in cardiovascular risk while examining lipids as markers of injury and repair. Participants will review the evidence surrounding statin therapy, hormone optimization for both men and women, and the impact of estradiol, testosterone, thyroid function, and targeted nutritional supplements on cardiovascular health and disease prevention.

Faculty: Clifford Gluck, MD, FACS

2:30 - 2:45 pmBreak
2:45 - 4:15 pmCardiovascular Disease: Beyond Cholesterol to Root Cause, Continued
4:15 - 4:30 pmBreak
4:30 - 5:00 pmInteractive Quiz
5:00 - 5:30 pmPanel Discussion and Q&A
Time (MT)Agenda
8:00 - 9:00 amObstructive Sleep Apnea: More Than a Sleep Disorder
Obstructive sleep apnea is closely linked to obesity, insulin resistance, and metabolic dysfunction, contributing to increased cardiovascular risk and chronic disease progression. This session examines the physiologic effects of intermittent hypoxia, elevated cortisol, and visceral adiposity while reviewing the potential role of progesterone in women with sleep-disordered breathing. Participants will also learn how to interpret common laboratory findings, including hemoglobin, hematocrit, and oxygen saturation, to better identify and manage patients at risk.

Faculty: Scott Davis, MD

9:00 - 9:15 amBreak
9:15 - 11:15 amBrain Health and Cognitive Aging: A Hormone-Centered Approach
Increasing evidence supports the concept that Alzheimer's disease may represent a form of "Type 3 Diabetes," linking insulin resistance, metabolic dysfunction, inflammation, and vascular disease to cognitive decline. This session explores the growing body of literature connecting hormones, brain metabolism, and healthy aging while examining the roles of testosterone, estradiol, progesterone, and other endocrine factors in preserving cognitive function. Participants will also review the evidence surrounding hormone therapy, and practical strategies to support brain health and reduce the risk of dementia and depression.

Faculty: Scott Davis, MD

11:15 - 12:30 pmBone, Muscle, and Structural Integrity: A Hormone-Centered Approach
Bone and muscle health are essential to healthy aging and play a critical role in preventing frailty, fractures, disability, and loss of independence. This session explores osteoporosis and sarcopenia as interconnected metabolic diseases influenced by hormonal decline, inflammation, and the balance between anabolic and catabolic processes. Participants will review the roles of estradiol, testosterone, and DHEA in maintaining skeletal and muscle integrity, examine the effects of common medications on bone health, and evaluate the evidence supporting nutritional supplements, and hormone optimization to preserve strength, mobility, and long-term function.

Faculty: Kristi Hales, RPH

12:30 PMAdjourn
In support of improving patient care, this activity has been planned and implemented by The Foundation for Care Management (FCM) and Worldlink Medical (WLM). FCM is jointly accredited by the Accreditation Council for Continuing Medical Education (ACCME), and the American Nurses Credentialing Center (ANCC), to provide continuing education for the healthcare team.
 
This program is approved for 19.75 AMA Category 1 Credits TM 
This program is approved for 19.75 Nursing contact hours of education. 
 
Healthcare provider should only claim credit commensurate with the extent of their participation in this activity
 
This activity was planned by and for the healthcare team, and learners will receive 19.75 Interprofessional Continuing Education (IPCE) credit for learning and change.
 

Location and Travel Details

  • Nov 6-8, 2026
  • Hyatt Regency
    170 South West Temple
    Salt Lake City, UT 84101
  • Salt Lake City International Airport (SLC)
  • Accommodations
    Block Rate $189
    Rate Expires 10/15/2026
    Book a Room

Pricing

  Early Bird
(up to 3 weeks prior to event)
Standard
(within 3 weeks of event)
Prescribers

This rate applies to licensed medical professionals who prescribe hormone therapy. Applicable credentials include MD, DO, PA, NP, and ND.
$1,595 $1,695
Non-Prescribers

Ideal for clinical support staff, students, and Legacy BHRT Series alumni seeking to refresh their knowledge. Applicable credentials include MA, RN, RPh, Resident / Intern, Pharmacist, Office Manager, Dietician, Nutritionist, and Health Coach.
N/A $1,095


NOTE: The course material is the same for both provider types.

Policies

Course Content Access

This training is offered both in person and virtually. Educational materials and the syllabus will be available online. A recording of each day’s session will be posted that evening and remain accessible until the second Sunday (2 weeks after the event) following the event, giving you time to review material or catch up on any missed sessions. Recordings will no longer be available after that date.

Group Discounts

If two or more prescribers register as a group under one registration ticket, there will be a 10% discount applied to each registration after the first one.

Refunds, Cancellations, and Course Credit

Up to 3 weeks prior to the course start date the cancellation fee is $100. If a cancellation is requested less than 3 weeks in advance the cancellation fee is $350. If a cancellation is received within two weeks of the event, there are no refunds allowed.

To cancel a registration, a credit can be held on file without penalty so long as the cancellation is received more than 2 weeks in advance of the start date. This credit will be applied automatically to your next registration before a credit card is charged.

Dates:
Nov 6-8, 2026 Jul 23-25, 2027 Salt Lake City, UT In Person / Virtual $1095.00 - $1595.00 Register Now